Wakeman Catherine A, Winkler Wade C
Department of Biochemistry, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
Methods Mol Biol. 2009;535:115-33. doi: 10.1007/978-1-59745-557-2_8.
RNA sequences fold in a hierarchical manner to form complex structures. This folding pathway proceeds first with formation of secondary structure elements followed by the compilation of tertiary contacts. Although bioinformatics-based tools are commonly used to predict secondary structure models, it is notoriously difficult to achieve a high degree of accuracy via these approaches alone. Therefore, a diverse assortment of biochemical and biophysical techniques are regularly used to investigate the structural arrangements of biological RNAs. Among these different experimental techniques are structural probing methods, which are often times employed to determine which nucleotides for a given RNA polymer are paired or unpaired. Yet other probing methods assess whether certain RNA structures undergo dynamical structure changes. In this chapter we outline a general protocol for in-line probing, a method for analyzing secondary structure (and backbone flexibility) and describe a basic experimental protocol for hydroxyl radical footprinting as a method of investigating RNA folding.
RNA序列以分层方式折叠形成复杂结构。这种折叠途径首先是二级结构元件的形成,随后是三级接触的组装。虽然基于生物信息学的工具通常用于预测二级结构模型,但仅通过这些方法很难达到高度的准确性。因此,经常使用各种各样的生化和生物物理技术来研究生物RNA的结构排列。在这些不同的实验技术中,有结构探测方法,这些方法经常用于确定给定RNA聚合物中的哪些核苷酸是配对的或未配对的。还有其他探测方法评估某些RNA结构是否经历动态结构变化。在本章中,我们概述了一种用于在线探测的通用方案,这是一种分析二级结构(和主链灵活性)的方法,并描述了作为研究RNA折叠方法的羟基自由基足迹法的基本实验方案。